Core to shell switching of the conduction channel on SnO2 nanowire sensors.

A sensor based on random connections of single-crystalline SnO2 nanowires (NWs) has been fabricated for ethanol detection. The NW length of ∼10 µm leads to the formation of several random node connections between the Ag electrodes. The samples were subjected to thermal treatments under a reducing atmosphere of H2/Ar, to generate oxygen vacancies at the surface of the NWs. As a result, the core conduction channel of the NWs, where the conduction is based on electron hopping through the potential barriers at the contact nodes, switch to the surface of the NWs by the creation of an impurity band of shallow donors located at 0.347 eV below the conduction band. We suggest that the H2-rich atmosphere of the thermal treatments induced the formation of interstitial hydrogen (H i ) and substitutional hydrogen (HO), which are shallow donors with low formation energy.

Evidence of multi-walled carbon nanotube fragmentation induced by sonication during nanotube encapsulation via bulk-suspension polymerization.

The synthesis of multi-walled carbon nanotube/polystyrene composites, with nanotube concentrations of 0.04, 0.08 and 0.16 wt%, was carried out by in situ bulk-suspension polymerization with the assistance of sonication. By using this method both encapsulation and exfoliation of the nanotubes into the polymer host were achieved. Evidence of significant nanotube fragmentation was found by scanning electron microscopy; the cause of such fragmentation was attributed to the induction of strong cavitation due to the application of ultrasound during the synthesis. Infrared spectroscopy showed no evidence of the formation of covalent bonds between the nanotubes and the polystyrene during the process of synthesis. The thermal stability was not improved by the inclusion of the nanotubes, it was attributed to the low nanotube concentrations; however, composites glass transition temperature showed improvements.

Simplified route to multi-walled carbon nanotube synthesis by aerosol assisted chemical vapor deposition.

Uniform multi-walled carbon nanotubes (MWCNTs) were obtained decomposing toluene inside of fused silica tubing previously covered with Co oxide thin film. The two-step process, ruled successively in the same aerosol assisted chemical vapor deposition (AACVD) set up, constitutes a simplified route to the synthesis of MWCNTs. First, Co oxide thin film was deposited inside of fused silica tubing at 723 K, using a precursor solution of Co acetate in absolute methanol. After Co oxide deposition, the covered tubing was heated up to 1173 K under Ar flow, then a mist of toluene was injected inside the tubing, using also Ar as carrier gas, consequently MWCNTs were obtained in the internal wall of the tubing. The Co oxide film and the MWCNTs were analyzed by scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and atomic force microscopy (AFM). Uniform and very long MWCNTs (several tens of microm) with diameters around 20 to 100 nm were observed, with the advantage that the content of Co particles inside the nanotube was very low.